Canonical Allele Identifier: CA650290086
Gene: RAD50 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556970_132556971insC , CM000667.2:g.132556970_132556971insC GRCh38
NC_000005.9:g.131892662_131892663insC , CM000667.1:g.131892662_131892663insC GRCh37
NC_000005.8:g.131920561_131920562insC NCBI36
NG_021151.1:g.5047_5048insC
NG_021151.2:g.4994_4995insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2314_-168-2313insC ENSP00000492349.2:n.-168-2314_-168-2313insC
ENST00000638504.1:n.207-2314_207-2313insC
ENST00000638568.2:c.-169+497_-169+498insC ENSP00000491158.2:n.-169+497_-169+498insC
ENST00000639899.1:n.290-2314_290-2313insC
ENST00000640655.2:c.-168-2314_-168-2313insC ENSP00000491596.2:n.-168-2314_-168-2313insC
ENST00000651541.1:c.-208_-207insC ENSP00000498795.1:n.-208_-207insC
ENST00000378823.7:c.-355_-354insC ENSP00000368100.4:n.-355_-354insC
ENST00000416135.5:c.-169+497_-169+498insC ENSP00000389515.1:n.-169+497_-169+498insC
ENST00000533482.5:c.-355_-354insC ENSP00000431225.1:n.-355_-354insC
NM_005732.3:c.-355_-354insC NP_005723.2:n.-355_-354insC